Gene entry
ETFA
electron transfer flavoprotein subunit alpha
- Chromosome
- 15
- Cytoband
- 15q24.2-q24.3
- Variants (rsID)
- 16
ETFA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 15 (region 15q24.2-q24.3). Its official name is “electron transfer flavoprotein subunit alpha”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs143834701Benignsingle nucleotide variantMultiple acyl-CoA dehydrogenase deficiency
- rs1801591Benignsingle nucleotide variantMultiple acyl-CoA dehydrogenase deficiency
- rs80292319Benignsingle nucleotide variantMultiple acyl-CoA dehydrogenase deficiency
- rs140169311Conflicting interpretationssingle nucleotide variantMultiple acyl-CoA dehydrogenase deficiency
- rs184587113Conflicting interpretationssingle nucleotide variantMultiple acyl-CoA dehydrogenase deficiency|Glutaric acidemia type 2A
- rs119458969Likely pathogenicsingle nucleotide variantGlutaric acidemia IIa|Multiple acyl-CoA dehydrogenase deficiency
- rs119458971Pathogenicsingle nucleotide variantGlutaric acidemia IIa
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.